Home

Omron HBP-1300 User's Manual

image

Contents

1. battery Battery level Battery level LCD contents and operations Icon Fully charged The icon is lit j 9 The unit can be used The icon flashes E40 error not displayed 0 ZAN A sco The unit can be used 4 The icon flashes E40 error displayed The unit cannot be used 0 PREN leveliota If the unit is being continuously used the power will be IKE automatically turned off in 30 seconds Connecting the AC Adapter AC power Verify that the power outlet supplies the specified voltage and frequency 100 240 V AC 50 60 Hz Connect the AC adapter to the DC jack on the unit and the power outlet Note When the battery pack is installed If there is no problem with the following AC adapter DC jack Power outlet Battery And the icon does not flash contact OMRON HEALTHCARE 15 System Settings The system settings are divided into two modes Menu Mode and Utility Mode Menu Mode Menu Mode allows you to configure the Initial Inflation Pressure Value and Auscultation Mode settings Initial Inflation Pressure Value Auscultation Mode ovo MODE MEMORY O STOP STOPO 1 Press the MODE button P Fu e Initial Inflation Pressure Value setting screen appears Pr5 2 Press the 4 or p button to change the setting Press the lt q button to change the setting in the order 2
2. Do not connect the positive and negative terminals of the battery with a wire or other metal object Do not carry or store a battery with metal necklaces hairpins or other metal objects Use only the specified type of battery A Caution Do not touch the positive and negative terminals of the battery pack with a wire or other metal object If battery fluid comes into contact with the skin or clothes immediately rinse with water Non Invasive Blood Pressure NIBP measurement A Warning If a cuff is used on a patient with an infection treat the cuff as medical waste or disinfect before reuse If frequently performing NIBP measurement using a cuff over an extended period of time periodically check the patient s circulation In addition wrap the cuff as indicated in the cautionary points in this manual Do not connect the NIBP cuff or cuff joint to a luer lock adapter Do not bend cuff tube during inflation and deflation particularly after a change of body position Do not wrap the cuff on the following parts An upper arm on which intravenous drip or a blood transfusion is being performed An upper arm on which gt sensor IBP catheter or other instrument is attached An upper arm with a shunt for hemodialysis If measuring blood pressure with the cuff wrapped on the arm on the side of the body where a mastectomy was performed check the patient s condition AN Caut
3. AC adapter AC ADAPTER E1600 9063658 2 UK plug type AC ADAPTER UK1600 9994843 9 A Caution Only OMRON GS CUFF can be used with this device Features of the Product The OMRON HBP 1300 is an affordable professional blood pressure unit that is clinically proven accurate and provides fast reliable results and is easy to use Key features benefits look 5 cuffs available SS 12 to 18 cm S 17 to 22 cm M 22 to 32 cm L 32 to 42 cm XL 42 to 50 cm 12 to 50 cm arm circumference range Designed to be used on a table Motion stop function When body movement is detected the device stops deflation for 5 seconds Irregular pulse Indicator Helps identify changes in heart rate rhythm or pulse which may be caused by heart disease or other serious health issues Inflation Pressure Setting 4 options Auto 220 mmHg 250 mmHg 280 mmHg Last reading display function Auto Off Custom Rechargeable battery Large easy to read backlight display 11 Features Functions of Unit Front and back of unit START STOP button Power ON OFF MODE 2 MODE button Power ON Measure blood pressure Press when the power is off to tum on the power and start blood pressure measurement During inflation or measurement press to stop Power OFF Hold down at least 3 seconds to turn off the power Press to enter Menu Mode and configure various settings
4. Manual Taking the Measurement in Auscultation Stopping the MeastileMment su ardo Saa egentes Tu nent eade nada sear beko cala n hdd Displaying East Reading s e seno ls a ekran do lo atio aa da a ala MD LJ kab arolas kaJ Maintenance Maintenance Inspection and Safety Management Cleaning of the Device se cist A a rk RR KK ON a na ft aa EA ACGESSO eR Gheck Defore S6 uus dodi d SS A A A TA VAONA ka COEUR Kl lt TrouDleshoolhg as os la o ua Sor E o rus umo A mo fono Do kago Rist Of Error COGS wit T MT PISO OSA res etila Dua uo axle duka dreo duna ge Specifications Factory Default Settings kakao Se PROV Technical Specifications HBP 1300 Manufacturers sss bins ce sedcastceaseceesteczecnseodsisadsdvess Introduction Intended Use Medical Purpose The device is a digital monitor intended for use in measuring blood pressure and pulse rate in adult and pediatric patient population with arm circumference ranging from 12 cm to 50 cm from 5 inches to 20 inches Intended User This device should be used by a medical professional Patient Population This device is intended for use on adults and children of age 3 years and old
5. Professional Blood Pressure Monitor HBP 1300 e Instruction Manual e Mode d emploi e Gebrauchsanweisung e Manuale di istruzioni e Manual de instrucciones e Gebruiksaanwijzing e e Kullanim Kilavuzu cus o AR Please completely read this Instruction Manual before using the monitor for the first time Read this manual to ensure the safe and accurate use of the monitor AL for Healthcare IM HBP 1300 E 01 02 2013 5337346 6 Contents Introduction cto aen ko abt es na so na ka aka sa Ko kd a mM TIRETTI ra e rna ko e ES A o ras ade a Warbingscand Gaullons Sn LAM Using the Unit Components of the mikado ds duma audo Sao unuo laudo CUI ONS A Features of the PIO UC Sel var Ea a NAA Features RUNCIONSO UN dE aa aia Installing the Battery PACK 2c o e sa uu t peson Connecting the AC Adapters uu o o System Settings Menu ModE cras dico eas eed xe TTETT TTT Utlty MOD Non Invasive Blood Pressure NIBP Measurement Non Invasive Pressure Measurement Cuff Selection and Applying the Cuff to the Patient Taking the Measurement in
6. 3 seconds when a measurement result is displayed the measured data is cleared without being stored Note When the monitor is left idle for one minute the backlight will disappear 23 Maintenance Maintenance Inspection and Safety Management The HBP 1300 must be maintained to ensure functionality and to secure the safety of patients and operators Daily checks and maintenance should be performed by the operator page 25 In addition qualified personnel are necessary to maintain the performance and the safety and to conduct periodic inspections We recommend that the verification test be performed at least once a year Example of connection for pressure accuracy confirmation 1 Display the pressure accuracy confirmation screen as explained in Utility Mode on page 17 Display 0 in the pressure accuracy confirmation screen LI Display the pressure value 2 Connect the blood pressure monitor the calibrated reference pressure gauge and the cuff and inflation bulb 3 Check the pressure value of the blood pressure monitor and the pressure value of the calibrated reference pressure gauge Note Make sure that the blood pressure monitor reading is within 3 mmHg compared to the calibrated reference pressure gauge To rapidly deflate the cuff press the lt q button To repeat Pressure Accuracy Confirmation turn off the power and repeat the procedure from step 1 in Utility Mode o
7. 46 x 66 x 37 mm 1 81 x 2 60 x 1 46 inch W x H x D Battery 54 x 43 5 x 15 4 mm 2 13 x 1 71 x 0 61 inch W x H x D Weight Main unit Approx 0 52 kg not including accessories and options AC adapter Approx 0 2 kg Battery Approx 0 1 kg Display 7 segment LCD Protection Class Class II AC Adapter Internal powered equipment when operating with battery only Degree of Protection Type BF MDD Classification Class Power supply AC adapter Input voltage range AC 100 V to 240 V Frequency 50 60 Hz Output voltage range DC 6 V 5 Rated output current 1 6 A Rechargeable battery Type 3 6 V 1900 mAh Number of operation cycles when fully charged 300 Measurement conditions New battery fully charged Ambient temperature of 23 C 73 4 F Using M size cuff SYS 120 DIA 80 PR 60 Inflation setting AUTO e One 5 minute cycle consisting of cuff measurement time wait time 30 Environmental Conditions Operational temperature and Temperature range 10 to 40 C 50 to 104 F humidity Humidity range 30 to 85 RH not condensed Atmospheric pressure 700 to 1060hPa Storage and transportation Temperature range 20 to 60 C 4 to 140 F Humidity range 10 to 95 RH not condensed Atmospheric pressure 500 to 1060hPa Non Invasive Blood Pressure NIBP Measurement technology Oscillometric Measurement method Dynamic Linear Deflati
8. Do not use with a defibrillator Do not install the unit in the following locations Locations subject to vibration such as ambulances and emergency helicopters A location where there is gas or flame A location where there is water or steam A location where chemicals are stored Do not use at extremely high temperature high humidity or high altitude Use only within the required ambient conditions Do not subject the unit to intense shock Do not place heavy objects on the AC adapter cable or allow the unit to sit on the cord Clinical testing has not been conducted on newborn infants and pregnant women Do not use on newborn infants and pregnant women Do not plug in or unplug the AC adapter with wet hands A Caution Do not install the unit in the following locations EN Locations with dust salt or sulfur Locations directly exposed to sunlight for extended periods of time in particular do not leave in direct sunlight or near a source of ultraviolet light for extended periods as ultraviolet light will cause deterioration of the LCD Locations subject to vibration or shock Near heaters Do not use the unit near large equipment that uses a switching relay for power ON OFF Before use during use Warning The unit complies with the EMC standard IEC60601 1 2 As such it can be used simultaneously with multiple medical instruments However if instruments th
9. Immunity test Electrostatic discharge IEC60601 1 2 test level 6 kV contact Compliance level 6 kV contact Electromagnetic environment guidance Floors should be wood concrete or burst power supply lines power supply lines ESD 8 KV air 8 kV air ceramic tile If floors are covered with IEC 61000 4 2 synthetic material the relative humidity should be at least 30 Electric fast transient 2 kV for 2 kV for Mains power quality should be that of a typical commercial or hospital 50 60 Hz magnetic field IEC 61000 4 8 IEC 61000 4 4 1 kV for input 1 kV for input environment output lines output lines Surge 1 kV 1 kV Mains power quality should be that of IEC 61000 4 5 differential mode differential mode a typical commercial or hospital 2 kV 2 kV environment common mode common mode Voltage dips short lt 5 Ur 5 Ur Mains power quality should be that of interruptions and for 0 5 cycle for 0 5 cycle a typical commercial or hospital voltage variations on 40 U 40 U environment If the user of the power supply input lines a 1300 requires continued IEC 61000 4 11 for 5 cycles for 5 cycles operation during power mains 70 96 70 96 Ur interruptions itis recommended that for 25 cycles for 25 cycles the HBP 1300 be powered from an uninterruptible power supply 5 Ur 5 Ur battery for 5 sec for 5 sec Power frequency 3 A m 3 A m Power frequen
10. is used Measure circumference or patient s arm and ensure Ensure cuff is applied to a bare arm or very thin Cuff wrapped over thick clothing clothing Patient not seated heart level Ensure patient is seated feet flat on the floor cuff at Ensure before measurement taken patient has not Patient ate drank or exerted themselves recently had food caffeinated or alcohol beverages or exerted exercised in the last 30 minutes 27 List of Error Codes The alarm lamp flashes when a medium priority alarm occurs and lights steadily when a low priority alarm occurs To clear an alarm press any button lf a low priority alarm and a medium priority alarm occur at the same time the medium priority alarm is displayed If the alarms are the same priority level the error code of the alarm that occurred first is displayed However to prevent battery consumption when powered by battery a low battery error E40 error is always given priority Example E2 mp La SYSTEM Error fe SS Priority Description Points to check code E9 Medium Internal hardware error Contact OMRON HEALTHCARE NIBP Error AUR Priority Description Points to check code The cuff tube is not connected Firmly connect the cuff tube E1 Low i Air is leaking from the cuff Replace with an OMRON GS CUFF that does not leak Did not inflate properly becau
11. where they purchased this product or their local government office for details of where and how they can take this item for environmentally safe recycling Business users should contact their supplier and check the terms and conditions of the purchase contract This product should not be mixed with other commercial wastes for disposal This product does not contain any hazardous substances Disposal of used batteries should be carried out in accordance with the national regulations for the disposal of batteries 32 Manufacturer s Declaration The HBP 1300 is intended for use in the electromagnetic environment specified below The customer or the user of the HBP 1300 should assure that it is used in such an environment Electromagnetic Emissions IEC60601 1 2 Emission Test Compliance Electromagnetic Environment RF emission Group 1 The HBP 1300 uses RF energy only for internal functions CISPR 11 Therefore this RF emission is extremely weak and there is little chance of it creating any kind of interference whatsoever with nearby electronic equipment RF emissions Class B The HBP 1300 is suitable for use in all establishments CISPR 11 including domestic establishments and those directly Class A ekagis to KI o supply network IEC 61000 3 2 at supplies buildings used for domestic purposes Voltage fluctuations flicker Complies IEC 61000 3 3 Electromagnetic Immunity IEC60601 1 2
12. 80 250 220 AUTO 280 Press the gt button to change the setting in the order 220 250 280 AUTO 220 When the Initial Inflation Pressure Value is set inflation takes place at a fixed speed to the set value and thus is quicker AUTO estimates the systolic blood pressure during inflation and automatically inflates the cuff to a suitable value When using 220 250 or 280 mmHg select the value that is 30 to 40 mmHg higher than the estimated systolic blood pressure 3 When you have completed the Initial Inflation Pressure Value setting press the MODE button LJ The Auscultation Mode settings screen appears F ON or OFF appears 4 Press the or p button to set to ON or OFF When set to ON SYS and DIA can be recorded using auscultation measurement For information on auscultation measurement see page 22 5 When you have completed the Auscultation Mode setting press the MODE button 0 appears To start blood pressure measurement press the START STOP button Note The body movement detection function is disabled while Auscultation Mode is in use If the power is turned off the settings revert to the factory settings Initial Inflation Pressure Value changes to AUTO and Auscultation Mode changes to OFF 16 Utility Mode Utility Mode allows you to co
13. If held down at least 3 seconds when a Measurement result is displayed the measured data is cleared without being stored in memory 3 4 1L p button Alarm lamp Displays the system settings page 16 and the last reading page 23 When using Auscultation Mode inflates and deflates the cuff Lights up or flashes when an alarm occurs page 28 NIBP connector Connects the cuff tube DC jack Battery cover NI O oc A Connects the AC adapter Open to install or replace the battery Meaning of the Symbols Symbol Description Symbol Description e This shows the Type BF applied part Consult the instruction manual Class Adapter 12 LCD Display ggedBB LILI ano LILII I ARN 3 8 21 7 C L namo mredi Ws df AEX 220 t 3 Co d 10 1 SYS Displays systolic blood pressure 2 DIA Displays diastolic blood pressure Pulse Displays the pulse rate 4 Pulse Flashes in synchronization with the pulse during synchronization icon measurement 5 Irregular pulse wave icon Lights in the measurement result display and memory display if the pulse wave interval was irregular or there was body movement during measurement page 23 6 EZ Memory icon Lights while the previous data are being displayed page 23 Charge icon Fla
14. MEE 80 MHz to 800 MHz 800 MHz to 2 5 GHz 4 1 2 d 1 2 2 3 0 01 0 12 0 12 0 23 0 1 0 38 0 38 0 73 1 12 12 23 10 3 8 3 8 7 3 100 12 12 23 For transmitters rated at a maximum output power not listed above the recommended separation distance d in metres m can be determined using the equation applicable to the frequency of the transmitter where is the maximum output power rating of the transmitter in watts W according to the transmitter manufacturer Note1 At 80MHz and 800MHz the separation distance for the higher frequency range applies Note2 These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people 35 Manufacturer E EU representative ec rer Production facility Subsidiary OMRON HEALTHCARE Co Ltd 53 Kunotsubo Terado cho Muko Kyoto 617 0002 JAPAN OMRON HEALTHCARE EUROPE B V Scorpius 33 2132 LR Hoofddorp THE NETHERLANDS www omron healthcare com OMRON DALIAN CO LTD Dalian CHINA OMRON HEALTHCARE UK LTD Opal Drive Fox Milne Milton Keynes MK15 ODG U K OMRON MEDIZINTECHNIK HANDELSGESELLSCHAFT mbH Gottlieb Daimler Strasse 10 68165 Mannheim GERMANY www omron medizintechnik de OMRON SANT FRANCE SAS 14 rue de Lisbonne 93561 Rosny sous Bois Cedex FRANCE Made in China
15. NIBP Measurement Non Invasive Pressure Measurement Principles Oscillometric method The beat in the pulsation generated by the contraction of the heart is captured as the pressure inside the cuff to measure the blood pressure If the cuff wrapped around the upper arm is pressurized sufficiently the blood flow stops but the beat of the pulsation is present and the pressure inside the cuff receives this and oscillates Next as the pressure inside the cuff gradually decreases the oscillation of the pressure within the cuff gradually increases and reaches a peak As the pressure within the cuff decreases further the oscillation decreases from its peak The pressure within the cuff and the relationship with the increase and decrease of the oscillation within the cuff in this series of processes are stored into memory calculations are carried out and the blood pressure value is determined The pressure within the cuff when the oscillation increases drastically is the systolic pressure and the pressure within the cuff when the oscillation decreases drastically is the diastolic pressure Also the pressure within the cuff when the oscillation peaks is taken as the average pulsation pressure The oscillometric method does not determine the blood pressure value instantly like a microphone type automatic blood pressure gauge with the auscultation method but rather determines it from the series of change curves as explained above Therefore it is not eas
16. at generate noise such as an electric scalpel or a microwave therapy device are near the unit check the operation of the unit during and after use of these instruments If an error occurs or a measurement result is questionable check the vital signs of the patient by auscultation or palpation Avoid relying solely on the measurement results of the unit when judging the patient s condition Only trained healthcare providers should use this device Do not allow patients to operate this device Properly connect the connectors and AC adapter cable Do not place objects or liquids on top of this unit Check the following before using the unit Make sure the AC adapter cable is not damaged wires are not exposed or broken and the connections are firm For the AC adapter connected to the unit supplies and optional devices use only the standard accessories or OMRON specified products Do not use in a location with moisture or a location where water may splash on the unit This unit is intended for use in physicians office hospitals clinics and other medical facilities Do not use the unit if it emits smoke an abnormal odor or abnormal noise Do not bring cellular telephones or transceivers into the room where the unit is installed or being used Do not connect multiple monitors to the same patient Do not connect the unit to a power outlet that is controlled by a wall switch AN Caut
17. ave or gas sterilization EOG formaldehyde gas high concentration ozone etc If using an antiseptic solution for cleaning follow the instructions of the manufacturer Clean the unit regularly Maintenance and inspection A Warning To use the unity safely and correctly always inspect the unit when starting work Unauthorized modification is prohibited by law Do not attempt to disassemble or modify the unit Warnings and cautions for safe measurement Rechargeable battery Warning If battery fluid comes in contact with the eye immediately flush with copious amounts of water Do not rub Seek medical attention immediately Do not use the battery pack in any other device besides this unit Do not throw into flame disassemble or heat Always disconnect the AC adapter from the unit before removing or installing a battery If the unit will not be used for a Month or longer remove the battery from the unit and store Charge the battery once every 6 months Storage conditions for the battery are a temperature of 20 to 30 4 to 86 F and a humidity of 65 12090 Before use always charge the battery Do not attempt to disassemble or modify the battery Do not apply pressure to and deform the battery Do not throw pound drop bend or hit the battery The battery has positive negative polarity If the battery does not connect well to the unit do not forcibly connect it
18. cy magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment Note is the a c mains voltage prior to application of the test level 33 80 AM 2Hz IEC60601 1 2 Compliance Electromagnetic Immunity test test level level environment guidance Portable and mobile RF communications equipment should be used no closer to any part of the HBP 1300 including cables than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter Recommend separation distance d 1 2 AP 150 kHz to 80 MHz 3 Vrms d 1 2 NP 80 MHz to 800 MHz Conducted 150 kHz to d 2 3 NP 800 MHz to 2 5 GHz IEC 61000 4 6 80 MHz 80 AM 2Hz where P is the maximum output power rating of the transmitter in watts W according to he transmitter manufacturer and d is the recom 3V mended separation distance in meters m m os dec 3 V m Field strengths from fixed RF transmitters as determined by an electromagnetic site survey should be less than the compliance level in each frequency range Interference may occur in the vicinity of equipment marked with the following symbol Note1 At 80 MHz and 800 MHz the higher frequency range Note2 These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and peo
19. e height as the right atrium of the heart 20 A Caution Make sure the cuff is wrapped in the correct arm position and is at the same height as the heart A difference of 10 cm 4 inches in height may cause a variation in the blood pressure value of up to 7 8 mmHg Note f measurement is difficult due to arrhythmia use a different blood pressure measurement method If the patient has acute inflammation a pyogenic ailment or an external wound at the location where the cuff is to be wrapped follow the instructions of the doctor Non Invasive Blood Pressure NIBP measurement is performed by compressing the upper arm Some people may experience intense pain or transient spotting caused by subcutaneous hemorrhaging may appear The spotting will disappear over time however if it is possible that this will disturb the patient try the following technique Wrap a thin towel or cloth one layer under the cuff If the towel or cloth is too thick there will be insufficient cuff compression and the blood pressure value will measure high If the patient moves or the cuff is touched this may be falsely detected as a pulse and over inflation will occur Do not inflate the cuff when it is not wrapped on the upper arm This may damage the cuff Taking the Measurement in Manual Mode 1 Press the START STOP button Blood pressure measurement is performed once 2 The measurement results are displayed If a measurement valu
20. e is outside the corresponding range below the value will flash SYS 59 mmHg or less or 251 mmHg or higher DIA 39 mmHg or less or 201 mmHg or higher PULSE 39 bpm or less or 201 bpm or higher Normal measurement Measurement error failure B8B Ji El 23 Ng Li me eJdB EA 3 A Caution The accuracy of a flashing measurement value that is outside the measurement range is not guaranteed Always check the patient s condition before deciding what steps to take Note If inflation is insufficient inflation may restart automatically while measurement is in progress 21 Irregular pulse wave detection function If the pulse wave interval becomes irregular during measurement the irregular pulse wave detection icon will light to notify you Body movement detection function If body movement is detected during measurement deflation stops for 5 seconds The irregular pulse wave icon appears in the measurement result display Deflation stopped After 5 seconds measurement resumes and an attempt is made to complete measurement in one cycle Taking the Measurement Auscultation Mode Use a stethoscope to perform measurement When set to ON SYS and DIA can be recorded using auscultation measurement To determine SYS and DIA during measurement press the MODE button SYS is registered the first time and DIA is registered the second time you press the MODE button during d
21. e manual for each optional accessory This manual does not contain cautionary information for optional accessory Exercise caution with the cables and arrange so that the patient does not become entangled or bound Before use during use Check the following after turning on the power No smoke abnormal odor or abnormal noise is emitted Press each button and verify that it operates For functions that cause icons to light or flash verify that the icons light or flash page 13 Measurement can be performed normally and measurement error is within the tolerance value If the screen is not displayed normally do not use the unit When recycling or disposing of parts including batteries of the unit follow local government rules and regulations Cleaning For cleaning see page 24 Rechargeable battery To prevent accidents keep batteries out of reach of infants and small children If you sense that something is wrong with a battery immediately move it to a safe location and contact the administrator responsible for the unit or OMRON HEALTHCARE If the battery voltage is low operation by battery may not be possible Non Invasive Blood Pressure NIBP measurement f the patient has acute inflammation a pyogenic ailment or an external wound at the location where the cuff is to be wrapped follow the instructions of the doctor Non Invasive Blood Pressure measurement NIBP is performed by compress
22. eflation After DIA is determined the cuff rapidly deflates and SYS and DIA are displayed as the measurement results The pulse rate does not appear in the measurement result display During deflation the UJ button can be held down to re inflate or the lt button can be held down to deflate faster Stored data that was measured in Auscultation Mode is displayed when the auscultation icon is lit B During re inflation Note The body movement detection function is disabled while Auscultation Mode is in use For Auscultation Mode settings see page 16 22 Stopping the Measurement To stop measurement while measurement is in progress press START STOP button Displaying Last Reading The previous measurement value systolic blood pressure diastolic blood pressure and pulse rate and whether or not an irregular pulse wave was detected can be displayed the case of auscultation measurement the auscultation icon appears Press the lt q button to display the previous data This function is also available when the device is switched off s 90 If an irregular pulse wave or i L LI body movement was detected DIA 1 the irregular pulse wave icon ilaj Li appears Lights while the previous PULSE min data are being displayed When the data was measured in Auscultation Mode the auscultation icon appears MODE MEMORY 000 GE If held down at least
23. er Environment The instrument is designed for use in physicians offices hospitals clinics and other medical facilities Measurement Parameter Non Invasive Blood Pressure Bi Pulse rate Precautions for Use Warnings and cautions described in the instruction manual should be observed at all times Exemptions OMRON will not bear any responsibilities on the following matters 1 When a problem or damage occurs caused by the maintenance and or repair conducted by a person other than OMRON or the dealer specified by OMRON 2 The problem or damage of OMRON product caused by the product of other manufacturer not delivered by OMRON 3 The problem and damage caused by the maintenance and or repair using the repair parts not specified by OMRON 4 The problem and damage caused by the results not observing the Notes on Safety or the operational method mentioned in this Instruction Manual 5 Under the circumstances not within the operating conditions of this unit including the power source or the setting environment mentioned in this Instruction Manual 6 The problem and damage caused by the result s of remodeling or improper repair of this product 7 The problem and damage caused by act of god such as fire earthquake flood or lightning 1 The contents of this Instruction Manual may be changed without prior notice 2 We have thoroughly reviewed the contents of this Instruction Manual However if an inadequate descriptio
24. es are not deformed due to falling or other impact The device is not dirty The device is not wet AC adapter The AC adapter is firmly connected to the connector on the device There are no heavy objects lying on the AC adapter cable The AC adapter cable is not damaged core wire exposure breaks etc When turning on the power When turning on the power check the following Display lamp When the START STOP button is pressed to turn on the power the screen below appears and the alarm lamp lights page 13 gt The alarm lamp is lit up SYS mmHg LO LI E Lir DIA mmHg PULSE min After turning on the power After turning on the power check for the following External appearance There is no smoke or odor coming from the device The device is not making any unusual noises Buttons Press each button and check that it works Non invasive blood pressure NIBP Make sure that a suitable OMRON GS CUFF is attached one that fits the circumference of the patients arm The cuff tube is firmly connected E The person checking the cuff should wrap the cuff around arm perform cuff measurement and check to see that blood pressure is in the vicinity of normal measurements While measurement is in progress bend the relevant arm and move body to halt discharge and during this halt check that cuff pressure does not drop 25 Troubleshoot
25. he aim to prevent unsafe product situations the EN60601 1 2 2007 standard has been implemented This standard defines the levels of immunity to electromagnetic interferences as well as maximum levels of electromagnetic emissions for medical devices This medical device manufactured by OMRON HEALTHCARE conforms to this EN60601 1 2 2007 standard for both immunity and emissions Nevertheless special precautions need to be observed Do not use mobile cellular telephones and other devices which generate strong electrical or electromagnetic fields near the medical device This may result in incorrect operation of the unit and create a potentially unsafe situation Recommendation is to keep a minimum distance of 7 m Verify correct operation of the device in case the distance is shorter Further documentation in accordance with EN60601 1 2 2007 is available within this manual refer to section Manufacturer s Declaration Correct Disposal of This Product Waste Electrical amp Electronic Equipment This marking shown on the product or its literature indicates that it should not be disposed with other household wastes at the end of its working life To prevent possible harm to the environment or human health from uncontrolled waste disposal please Emm separate this product from other types of wastes and recycle it responsibly to promote the sustainable reuse of material resources Household users should contact either the retailer
26. ily affected by external noise an electric scalpel or other electro surgical instruments KOROTKOV SOUNDS CUFF PRESSURE 200 OSCILLATIONS IN CUFF PRESSURE RADIAL PULSE 5 SEC Comparison between the auscultatory oscillometric and palpatory methods of measuring blood pressure L A Geddes The Direct and Indirect Measurement of Blood Pressure Year Book Medical Publishers Inc 1970 18 Cuff Selection and Connection Selecting the cuff A Warning Ifa cuff is used on a patient with an infection treat the cuff as medical waste or disinfect before reuse A Caution Do not use the cuff if it is damaged or has holes Use the appropriate cuff size to ensure correct measurements If a cuff that is too large is used the measured blood pressure value tends to be lower than the actual blood pressure If a cuff that is too small is used the measured blood pressure value tends to be higher Note It is important to use the correct sized cuff for a patient in order to get an accurate reading Measure the circumference of the patient s arm and select the cuff size that is appropriate for the circumference Select the cuff that is suitable for the patient from the cuffs below Arm circumference Cuff name inch GS CUFF XL 42 50 17 20 GS CUFF L 32 42 13 17 GS CUFF M 22 32 9 13 GS CUFF S 17 22 7 9 GS CUFF SS 12 18 5 7 Available as an opt
27. ing The power does not turn on Cause Solution If the unit is being powered by the battery the battery is not installed or tne charge is depleted Insert battery or replace with a new battery page 14 Disconnect the AC adapter remove the battery and contact OMRON HEALTHCARE e Check if the AC adapter is disconnected or the connection is loose e Check if the AC adapter or battery has failed Internal part failure The unit display does not operate Cause solution Stop using the unit and contact OMRON HEALTHCARE The unit becomes hot Cause Solution An object is on top of the unit or right next to the unit Keep the area around the unit free of objects If the unit becomes too hot to be touched there may be a problem in the unit Turn off the unit power disconnect the AC adapter remove the battery and contact OMRON HEALTHCARE The unit is connected to a power outlet but it runs on the the battery pack Cause solution power cannot be supplied the unit will operate by battery only e Check if the AC adapter is properly connected to the unit e Check if AC adapter is connected to a power outlet e Check that the electrical outlet is working by connecting a different device to the same power outlet The cuff does not inflate when the START STOP button is pressed Cause Solution Loose cuff tube connection Check the connecti
28. ing the upper arm Some people may experience intense pain or transient spotting caused by subcutaneous hemorrhaging bruising may appear The spotting will disappear with time however it may be appropriate to inform patients for whom this may be a concern that spotting sometimes occurs and if necessary refrain from measurement To measure correctly it is recommended that the patient relax and not talk during measurement EN To measure correctly it is recommended that the patient rest quietly for 5 minutes before measurement Using the Unit Components of the Product Before using the unit make sure that no accessories are missing and that the unit and accessories are not damaged If an accessory is missing or there is damage please contact OMRON HEALTHCARE Main unit Standard Medical Accessories GS CUFF L 32 42 cm M 22 32 cm AC adapter Others Battery pack Instruction Manual this paper Options Optional Accessory Battery pack HXA BAT 2000 9065797 0 10 Optional Medical Accessories within the scope of EC Medical Device Directive 93 42 EEC GS CUFF XL GS CUFF L GS CUFF M GS CUFF S HXA GCUFF XLLB HXA GCUFF LLB HXA GCUFF MLB HXA GCUFF SLB 9065802 0 9065798 9 9065799 7 9065800 4 CUFF HOSE No 1 3 5m HBP CUFFH BLU35 9968171 8 CUFF HOSE No 2 1 5m HBP CUFFF BLU15 9968172 6 GS CUFF SS HXA GCUFF SSLB 9065801 2
29. ion Before using the unit verify that none of the following apply to the patient Poor peripheral circulation noticeably low blood pressure or low body temperature there will be low blood flow to the measurement position The patient uses an artificial heart and lung there will be no pulse An SpO sensor and the cuff are attached to the same arm The patient has an aneurysm The patient has frequent arrhythmia Body motions such as convulsions arterial pulsations or trembling cardiac massage in progress minute continuous vibrations rheumatism etc Before use visually inspect the unit to make sure there are no deformations due to falling and that there is no dirt or moisture on the unit When the unit has not been used for an extended period of time always verify that it operates normally and safely before use Do not use in a location where the unit may easily fall In the event that the unit falls verify that it operates normally and safely Cleaning Warning When cleaning the unit turn off the power and disconnect the AC adapter from the unit After cleaning the unit make sure it is completely dry before connecting to a power outlet Do not spray pour or spill liquids into or onto the unit accessories connectors buttons or openings in the housing AN Caution Do not use thinner benzene or other solvents to clean the unit Do not sterilize by autocl
30. ion NIBP measurement should be performed on the upper arm During NIBP stop excessive body movement by the patient and minimize trembling Ifa doctor has indicated that the patient has hemorrhagic diathesis or hypercoagulability check the condition of the arm after measurement Use the appropriate cuff size to ensure correct measurements If too large a cuff is used the measured blood pressure value tends to be lower than the actual blood pressure If too small a cuff is used the measured blood pressure value tends to be higher Before and during measurement verify that none of the following apply to the patient The part where the cuff is wrapped is at a different height than the heart A difference of 10 cm 4 inches in height may cause a variation in the blood pressure value of up to 7 or 8 mmHg Body movement or conversing during measurement Cuff wrapped over thick clothing Pressure on the arm due to a rolled up sleeve In the case of a cuff for adults the cuff should be wrapped to a tightness that allows two fingers to be inserted in between the cuff and the arm The accuracy of a flashing measurement value that is out of the measurement range cannot be guaranteed Always check the patient s condition before deciding what steps to take Do not use the cuff if it is damaged or has holes Only OMRON GS CUFF can be used with this device Note Setup Read and understand th
31. ional accessory Connecting the cuff EN Connect the cuff tube to the NIBP connector on the unit and turn clockwise to lock AN Caution Only OMRON GS CUFF can be used with this device Note If the cuff tube is too short the optional 3 5 m or 1 5 m CUFF HOSE can be connected to lengthen the cuff tube Do not extend other than the optional 3 5 m or 1 5 m CUFF HOSE as this will affect measurement accuracy Make sure the connections are tight 19 Applying the Cuff to the Patient 1 Wrap a bare arm or over thin clothing Wrap the cuff on a bare arm or over thin clothing Thick clothing or a rolled up sleeve will cause inaccurate blood pressure measurements The device can be used on either the right or left arm lt 2 Align the artery mark INDEXY ARTERY with the brachial artery Run the cuff tube out the peripheral side with no bends the brachial artery is on the inner side of the patient s upper arm Make sure that INDEX W ARTERY is within the RANGE and the lower edge of the cuff is 1 to 2 cm from the inner side of the elbow joint If INDEX W ARTERY is outside the RANGE error in the blood pressure value will increase In this case use a different cuff size As a guideline for the tightness of the cuff It should be possible to insert about two fingers under the cuff 3 During measurement keep the brachial artery on which the cuff is wrapped at the sam
32. n or error is found please let us know 3 It is prohibited to copy a part of or the entire Instruction Manual without getting OMRONV s permission Unless this Instruction Manual is used by an individual company it cannot be used without getting OMRON s permission from the standpoint of the Copyright Law Notes on Safety The warning signs and symbol examples indicated below are intended to ensure safe use of the product and prevent damage and injury to you and others The signs and symbols are explained below Safety Symbols used in this Instruction Manual 2 Indicates the matters in which death or severe bodily damage may arise as a result A Warning of incorrect handling Indicates the matters in which bodily harm or material damage may arise as a result AN Caution of incorrect handling General Information Note indicates general information to keep in mind when using the unit and other useful information Warnings and Cautions Usage warnings and cautions Setup A Warning Do not use the cuff or AC adapter to lift the unit it can also cause the unit to malfunction If the unit has broken down contact OMRON HEALTHCARE Do not use in combination with a hyperbaric oxygen therapy device or in an environment where combustible gas may be generated Do not use in combination with magnetic resonance imaging MRI equipment MRI is to be performed remove cuff connected to the unit from the patient
33. n page 17 Cleaning of the Device Cleaning and disinfecting should be performed in accordance with your facility s infection control practice Surface cleaning Wipe with a cloth that has been moistened with isopropyl alcohol diluted to 50 v v or ethyl alcohol disinfection alcohol diluted to 80 v v or less and wrung out Do not wipe the DC jack or allow it to become wet Removing dust Use a moistened cotton bud to remove dust that has accumulated on the vent ports Service The device requires no routine service other than cleaning and visually checking the cuffs tubing etc AN Caution Do not sterilize by autoclave or gas sterilization EOG formaldehyde gas high concentration ozone etc If using an antiseptic solution for cleaning follow the instructions of the manufacturer Accessory Care Non Invasive Blood Pressure Measurement NIBP Cuff Wipe clean on the surface of the cuff with a cloth moistened with a 70 v v dilution of isopropyl alcohol or a 80 v v or less dilution of disinfection ethanol ethyl alcohol Do not allow any liquids inside the cuff If a liquid gets in the cuff dry the inside well 24 Check before Use Before conducting safety checks be sure to implement the items in the Cleaning of the Device and Accessory Care sections page 24 Before turning on the power Before turning on the power check for the following External appearance The device or accessori
34. nfigure the Auto Power Off and Pressure Accuracy Confirmation setting MODE MEMORY EMO OGO 1 Confirm that the device is switched off If the power is on hold down the START STOP button for at least 3 seconds to turn off the power D on oan 2 Hold down the MODE button until the Auto Power Off setting screen appears The Initial Inflation Pressure Value setting screen appears and changes to the Auto Power Off setting screen appears a us pl 3 Press the lt or p button to change the auto power off 5 or 10 setting appears The 5 min or 10 min setting is entered When the unit is powered by the battery pack and is not used for the set time 5 min or 10 min the power automatically turns off to save battery power mid priority alarm other than a low battery error E40 error has occurred the power does not turn off automatically 4 When you have completed the Auto Power Off setting press the MODE button n EN The Pressure Accuracy Confirmation screen appears 0 appears LJ Nus appears 5 Check the Pressure Accuracy Add pressure externally as explained on page 24 Compare with the displayed value and verify that there is no problem 6 When you have completed Pressure Accuracy Confirmation press the START STOP button The power turns off 17 Non Invasive Blood Pressure
35. on There is an air leak in the cuff Replace the cuff If pressure is displayed the cuff tube is bent Make sure no part of the cuff tube is bent Measurement was not possible Cause solution Check the patient by palpation or other method After checking the patient check the error code and see List of Error Codes page 28 for Non Invasive Blood Pressure NIBP measurement 26 Abnormal measurement value Cause solution The causes below are possible Check the patient by palpation and then repeat measurement Body movement chills or other trembling Arrhythmia Noise in the cuff A nearby person touched the patient Cardiac massage was being performed The measurement value is questionable Cause Solution Deflates quickly Check for a loose cuff connection Stethoscope Simultaneously perform measurement with a stethoscope Place the stethoscope and listen while viewing the pressure display of the manometer an Blood pressure may vary widely due to physiological effects The causes below are possible Emotional excitement or agitation Pain due to cuff wrapping White coat hypertension Cuff size or wrapping method not correct Cuff wrapping position on upper arm not at the same height as the heart Patient s blood pressure not stable due to pulsus alternans respiratory changes or other reason Incorrect cuff size used correct sized cuff
36. on method Pressure display range 0 to 300 mmHg Pressure display accuracy Within 3 mmHg NIBP measurement range SYS 60 to 250 mmHg DIA 40 to 200 mmHg Pulse rate 40 to 200 min NIBP accuracy Maximum mean error within 5mmHg Maximum standard deviation within 8mmHg Pulse rate accuracy Within 5 96 of reading Reference standard EN1060 1 1995 A2 2009 EN1060 3 1997 A2 2009 ISO81060 1 2007 Comparison with auscultation method performed by a trained professional DIA determined by the auscultation method is K5 Note Specifications may be changed without prior notice C 0197 This blood pressure monitor fulfils the requirements of the EC directive 93 42 EEC Medical Device Directive It also conforms to the European standard EN 1060 Non invasive Sohygmomanometers Part 1 General Requirements and Part 3 Additional Requirements for Electromechanical Blood Pressure Measuring Systems 31 Important information regarding Electro Magnetic Compatibility EMC With the increased number of electronic devices such as PC s and mobile cellular telephones medical devices in use may be susceptible to electromagnetic interference from other devices Electromagnetic interference may result in incorrect operation of the medical device and create a potentially unsafe situation Medical devices should also not interfere with other devices In order to regulate the requirements for EMC Electro Magnetic Compatibility with t
37. ple 34 Field strengths from fixed transmitters such as base stations for radio cellular cordless telephones and land mobile radios amateur radio AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy To assess the electromagnetic environment due to fixed RF transmitters an electromagnetic site survey should be considered If the measured field strength in the location in which the HBP 1300 is used exceeds the applicable RF compliance level above the HBP 1300 should be observed to verify normal operation If abnormal performance is observed additional measures may be necessary such as reorienting or relocating the HBP 1300 Over the frequency range 150 kHz to 80 MHz field strengths should be less than 3 V m Recommended Separation Distances Recommended separation distance between portable and mobile RF communications equipment and the HBP 1300 The HBP 1300 is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled The customer or the user of the HBP 1300 can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment transmitters and the HBP 1300 as recommended below according to the maximum output power of the communications equipment Separation distance according to frequency of transmitter Rated maximum output m rero transmiter Masks
38. se the arm Have the patient not move the arm or body or body moved during measurement and repeat measurement Moved body or arm during Have the patient not talk or move and measurement or talked repeat measurement The cuff is not applied correctly Correctly apply the cuff The sleeve is rolled up and is E2 LOW Compressing the atm Remove the garment and re wrap the cuff The measurement time exceeds the expected time so the measurement was Measurement time has exceeded ey ended in order to avoid patient discomfort specified time ee AUN There is a possibility that measurement is Specified time 165 seconds being repeated over and over due to air leaking from the cuff 28 Other problems Error Priority Cause Solution code Inflated the cuff to 300 mmHg or more When inflating in Auscultation Mode 7 release the button when the pressure during inflation in Auscultation Mode reaches the desired value E3 L w If this occurs during measurement repeat measurement Over inflation occurs If this occurs when not performing measurement contact OMRON HEALTHCARE Recharge the battery or replace with a new E40 Medium The battery is depleted battery page 14 Try charging again If continues to fail E41 Medium Battery failed to charge newibarene pago 14 Replace the battery with a new battery If the E42 Medi
39. shes during charging Solid colored light displays when charging is finished Battery charge level icon Displays how much charge the battery has page 14 9 Qo Auscultation icon Lights when Auscultation Mode is ON page 16 10 eh a i Inflation setting icon The set initial Inflation pressure value lights page 16 Only when the battery is installed 13 Installing the Battery Pack Warning If battery fluid comes in contact with the eye immediately flush with copious amounts of water Do not rub Seek medical attention immediately Do not use the battery pack in any other device besides this unit Do not throw into flame disassemble or heat AN Caution Do not short the positive and negative terminals of the battery pack with a wire or other metal object If battery fluid comes into contact with the skin or clothes immediately rinse with water 1 Make sure the AC adapter has been disconnected 2 Remove the two screws from the top of the rear unit cover and remove the battery cover 3 Connectthe battery pack to the connector on the monitor and insert the battery pack into the compartment so that the triangle mark on the battery pack is aligned with the triangle mark on the monitor 4 Replace the battery cover and secure with screws Take care not to pinch the wires when replacing the cover 5 Connect the AC adapter to the unit and charge the battery pack When using
40. the battery pack for the first time be sure to fully charge about 4 hours before using Battery life About 300 measurements are possible with one charge A general guideline for replacement of the battery pack is about one year however the usage time per charge may grow shorter depending on usage conditions If you find that the usage time after each charge has grown shorter and the 4 icon frequently appears replace the battery pack Charging time Charging automatically starts after the AC adapter is connected When a new battery pack or a battery pack that has not been used for a long time is used some time may elapse before charging starts e The ___ icon flashes during charging Charging is completed in about 4 hours Low battery When the _ 4 icon starts flashing promptly charge the battery pack When the icon changes to f the battery is too low for blood pressure measurement Charge the battery Auto Power Off When the unit is powered by the battery pack the power automatically turns off after the set time elapses if you forget to turn off the power When the unit is used with the AC adapter connected the Auto Power Off setting does not operate 14 Battery charging State LCD contents and operations Icon Charging The icon flashes 2L Fully charged Charging completed Problem with the The icon is lit JL Error message is displayed
41. um Battery voltage error error continues contact OMRON HEALTHCARE Disposal Description As there is a risk of environmental pollution follow your applicable national and local legal regulations regarding disposal or recycling of this equipment and batteries The main constituents of each part are listed in the table below As there is a risk of infection do not recycle patient attachments such as cuffs but dispose of them as instructed by your facility s procedures and applicable regulations Item Parts Material Box Cardboard Package Cushion Cardboard Bag PE Main unit and Enclosure ABS PC SR accessories Internal parts General electronic components Outer tube PVC Battery pack Cell batteries Nickel metal hydride Internal parts General electronic components 29 Specifications Factory Default Settings Factory default settings and backup are as shown below Backup Setting is retained even if the power is interrupted Z Reverts to factory default setting if the power is turned off Setting Pressure Value Settings Factory Setting Backup Initial Inflation Pressure Value AUTO 220 250 280 AUTO A Auscultation Mode ON OFF OFF A Auto Power Off 5 min 10 min 5 min O Technical Specifications HBP 1300 Main unit Measurement Parameter NIBP PR Dimension Main unit 123 x 201 99 mm 4 84 x 7 91 x 3 90 inch W x H x D AC adapter

Download Pdf Manuals

image

Related Search

Related Contents

PA_R88.0  INSTRUCTIONS FOR USE FOR C  at y。ur Side  無停電電源装置(UPS) 取扱説明書  

Copyright © All rights reserved.
Failed to retrieve file